EP2551300B1 - Composition de résine, son procédé de production et structure multicouche - Google Patents

Composition de résine, son procédé de production et structure multicouche Download PDF

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Publication number
EP2551300B1
EP2551300B1 EP11759453.1A EP11759453A EP2551300B1 EP 2551300 B1 EP2551300 B1 EP 2551300B1 EP 11759453 A EP11759453 A EP 11759453A EP 2551300 B1 EP2551300 B1 EP 2551300B1
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EP
European Patent Office
Prior art keywords
evoh
resin composition
acid
component
ethylene
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German (de)
English (en)
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EP2551300A4 (fr
EP2551300A1 (fr
Inventor
Yoshikazu Yamasaki
Yasuhiro Nonaka
Kazuyuki Somemiya
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Kuraray Co Ltd
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Kuraray Co Ltd
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/306—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/092—Polycarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/04—Oxygen-containing compounds
    • C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/098—Metal salts of carboxylic acids

Definitions

  • the present invention relates to a resin composition, a method for production thereof and a multilayered structure including a layer obtained from the resin composition.
  • Ethylene-vinyl alcohol copolymers (hereinafter, may be also referred to as “EVOH”) are superior in oxygen barrier properties, transparency, oil resistance, antistatic properties, mechanical strength and the like, and thus have been widely used as various types of wrapping materials such as films, sheets, containers, etc.
  • EVOH is expected to have superior appearance characteristics in melt molding (being enabling molded products having superior appearances without generation of gels and seeds (dirt under paint), occurrence of coloring such as yellowing, and the like to be obtained), long-run workability (a property capable of obtaining a molded product without generation of fish eyes, streaks, etc. , due to no change of physical properties such as viscosity, etc., if molded for a long period of time), and the like.
  • films, sheets and the like are often formed with a multilayered structure having an EVOH layer for the purpose of improving oxygen barrier properties and the like.
  • a metal salt is often contained in an EVOH composition in order to improve adhesiveness between layers.
  • coloring such as yellowing is more likely to be caused, and thus appearance characteristics are deteriorated.
  • an edge part (trim) of a sheet after a molded product was obtained is recovered and reused, and there is a disadvantage that deterioration of the EVOH proceeds every time reuse is repeated, and defects such as gels and seeds increase whereby an appearance of a molded product is deteriorated.
  • melt molding may be carried out at a comparatively high temperature over 200°C in accordance with a melting temperature of the other resin.
  • melt molding is carried out at such a comparatively high temperature
  • conventional EVOH compositions have been disadvantageous in that yellowing, etc. is likely to occur.
  • molding thereof requires a high temperature, so that an EVOH is also exposed to a higher temperature such as e.g., no lower than 260°C. Therefore, an EVOH has been required which can prevent yellowing from occurring under such high temperatures.
  • JP 05-194805 A describes a thermoplastic resin including a saponified ethylene-vinyl acetate copolymer.
  • JP 10-067898 A discloses a saponified ethylene-vinyl ester copolymer composition and a multilayer coextrudate.
  • JP 2002-284886 A discloses a method for efficiently and stably manufacturing various kinds of ethylene/vinyl alcohol copolymers (EVOH's) in small quantities.
  • WO 2000/020211 A1 discloses a coextrusion multilayer structure comprising a layer of an ethylene/vinyl alcohol copolymer (EVOH) resin composition which contains a boron compound, a carboxylic acid and/or a salt thereof, and an alkali metal salt.
  • EVOH ethylene/vinyl alcohol copolymer
  • JP 2007-063428 A discloses an ethylene-vinyl alcohol copolymer resin composition and a method for producing the same.
  • the present invention was made in view of the circumstances described above, and an object of the present invention is to provide an EVOH-containing resin composition having superior appearance characteristics and long-run workability in melt molding and being capable of inhibiting occurrence of yellowing, etc., in melt molding, particularly in melt molding even at a high temperature of, for example, no lower than 260°C, and to provide a multilayered structure molded from the composition.
  • a further object of the present invention is to provide a method for producing the EVOH-containing resin composition.
  • One aspect of the present invention made to solve the foregoing problems provides a resin composition containing:
  • the resin composition of the present invention contains a multivalent carboxylic acid and/or a multivalent carboxylate ion as the component (B2) and a metal ion as the component (C), a multilayered structure superior in interlayer adhesiveness can be obtained, and further generation of gels, seeds or the like in melt molding can be inhibited, thereby resulting in an achievement of superior appearance characteristics and the long-run workability.
  • the multivalent carboxylic acid and the like are stably coordinated with the metal ion that is reportedly a cause of yellowing, etc. , thereby enabling an incorporation of the metal ion.
  • the resin composition the multivalent carboxylic acid and the like are stably present in a state of coordination with the metal ion as described above, so that a catalytic function that the metal ion has for reactions such as yellowing of the EVOH can be inhibited.
  • coloring such as yellowing can be inhibited in melt molding not only at a usually employed temperature, for example, no lower than 200°C, but also at a higher temperature, for example, no lower than 260°C.
  • the content of the component (B2) is preferably 0.01 ⁇ mol/g or greater and 20 ⁇ mol/g or less. According to the resin composition, due to the content of the component (B2) falling within the range, various characteristics such as a high inhibition property against yellowing in melt molding at a high temperature are enhanced.
  • the component (B2) preferably has at least one type of functional group selected from the set consisting of a hydroxy group, an amino group and a ketone group.
  • the component (B2) i.e., the multivalent carboxylic acid and/or the multivalent carboxylate ion has such functional groups
  • stability in a state where the component (B2) is coordinated with the metal ion is enhanced, so that an inhibition property of occurrence of coloring in melt molding of the resin composition at a high temperature, and the like can be enhanced.
  • a hydroxy group is favorable in that, for example, coordination strength with the metal ion can be adjusted appropriately, and a multilayered structure superior in interlayer adhesiveness is obtained whereas occurrence of coloring is inhibited.
  • At least a pair of carboxyl groups in the component (B2) are linked to each other via a linking group having 1 or 2 carbon atom(s). It is considered that the multivalent carboxylic acid and the like can be coordinated in a sterically stable manner with respect to one metal ion since at least a pair of carboxyl groups in the multivalent carboxylic acid and/or the multivalent carboxylate ion in the component (B2) is arranged with such an interval in the structure of the component (B2). Therefore, according to the resin composition, occurrence of coloring such as yellowing in melt molding at a high temperature can be further reduced. In addition, various characteristics such as the appearance characteristic, the long-run workability, adhesiveness between layers, etc. can be achieved in a well-balanced manner. It is to be noted that a carboxyl group herein includes also a carboxylate group in a carboxylate ion.
  • the component (B2) preferably has at least three carboxyl groups. Since a multivalent carboxylic acid and/or a multivalent carboxylate ion having at least three carboxyl groups can be coordinated with a metal ion in a more electrically and sterically stable and efficient manner, various functions such as an inhibitory function of occurrence of coloring in melt molding of the resin composition at a high temperature can be improved.
  • the content of the component (C) is preferably 2.5 ⁇ mol/g or greater and 22 ⁇ mol/g or less. According to the resin composition, due to the content of the metal ion as the component (C) falling within the range, the appearance characteristics are improved, and further the interlayer adhesiveness in molding a multilayered structure and the like can be enhanced.
  • the component (C) preferably includes (C1) an alkali metal ion (hereinafter, may be also referred to as "(C1) component”). Due to including an alkali metal ion in the component (C), the appearance characteristics are improved, and further the long-run workability, the interlayer adhesiveness in molding a multilayered structure, and the like are enhanced.
  • the content of the component (C1) is preferably 2.5 ⁇ mol/g or greater and 22 ⁇ mol/g or less.
  • the content of the alkali metal ion as the component (C1) falls within the range, the long-run workability and the interlayer adhesiveness when molded into a multilayered structure can be well balanced at a higher level.
  • the molar ratio (B2/C) of the component (B2) to the component (C1) is preferably 0.002 or greater and 2 or less. According to the resin composition, due to the molar ratio of the component (C1) to the component (B2) falling within the range, further higher inhibitory potential against coloring at a high temperature can be achieved whereas a balance between the long-run workability and the interlayer adhesiveness in molding a multilayered structure is maintained.
  • the component (C) also includes (C2) an alkaline earth metal ion (hereinafter, also referred to as "(C2) component").
  • (C2) component an alkaline earth metal ion
  • the appearance characteristic is improved, and further generation of gels or seeds is inhibited even when the multilayered structure including an EVOH layer is repeatedly recovered and reused, thereby resulting in inhibition of deterioration of an appearance of a molded product.
  • the resin composition preferably further contains (D) a phosphate compound (hereinafter, may be also referred to as "(D) component") and the content of the phosphate compound (D) is preferably 5 ppm or greater and 500 ppm or less in a value of phosphate radical.
  • a phosphate compound hereinafter, may be also referred to as "(D) component"
  • the content of the phosphate compound (D) is preferably 5 ppm or greater and 500 ppm or less in a value of phosphate radical.
  • the resin composition preferably further contains (E) a boron compound (hereinafter, may be also referred to as "(E) component") and the content of the boron compound (E) is preferably 50 ppm or greater and 2,000 ppm or less in a value of boron element. Also when the resin composition contains the boron compound falling within the range, thermal stability in melt molding is enhanced, thereby enabling further improvement in the appearance characteristics, etc.
  • (E) component a boron compound
  • the content of (B1) a monocarboxylic acid and a monocarboxylate ion as the component (B) (hereinafter, may be also referred to as "(B1) component”) is preferably less than 2 ⁇ mol/g.
  • the content of the monocarboxylic acid and the monocarboxylate ion as the component (B1) falls within the range, the appearance characteristics is improved, and further generation of an odor in molding and/or of a molded product can be inhibited.
  • the component (B) also preferably further includes the monocarboxylic acid and/or the monocarboxylate ion (B1), and the content of the monocarboxylic acid and the monocarboxylate ion (B1) is no less than 2 ⁇ mol/g.
  • the content of the monocarboxylic acid and the monocarboxylate ion as the component (B1) falls within the range, adjustment of quantities of the component (B) and the component (C) is facilitated in producing the resin composition, thereby enabling a stable production.
  • the resin composition can be suitably used in intended usage of co-extrusion molding due to having superior appearance characteristics and the long-run workability and can reduce occurrence of yellowing, etc. particularly in melt molding at high temperatures.
  • a method for producing the resin composition includes:
  • the mixing step is preferably carried out in a system in which the concentration of the vinyl ester is no greater than 1,000 ppm. According to the method, yellowing in melt molding of the obtained resin composition is inhibited, and further favorable color characteristics of the resin composition per se can be attained.
  • the method for producing the resin composition of the present invention further includes an pelletizing step in which a water-containing pellet of an ethylene-vinyl alcohol copolymer is obtained by an pelletizing operation from a solution including the ethylene-vinyl alcohol copolymer obtained in the saponifying step, and a drying step in which the water-containing pellet is dried to obtain a resin composition including an ethylene-vinyl alcohol copolymer, wherein the mixing step is carried out later than the pelletizing step. Also according to the method, a resin composition accompanied by reduced yellowing in melt molding can be obtained effectively.
  • the mixing step is carried out between the pelletizing step and the drying step by immersing the water-containing pellet in a solution containing the component (B2').
  • the component (B2') can be efficiently mixed in the resin composition, whereby a resin composition accompanied by inhibited yellowing in melt molding can be effectively produced.
  • the mixing step is carried out in the pelletizing step. According to the method, yellowing in melt molding of the obtained resin composition is reduced, and further favorable color characteristics of the resin composition per se can be attained.
  • the mixing step is preferably carried out in the saponifying step. According to the method, yellowing is reduced in melt molding when the resin composition of the present invention is obtained, and further favorable color characteristics of the resin composition per se can be attained.
  • a multilayered structure is provided with at least one layer obtained from the aforementioned resin composition.
  • the multilayered structure of the present invention has a superior appearance with inhibited occurrence of coloring such as yellowing, gels, seeds, and the like since the multilayered structure of the present invention is provided with a layer obtained from the resin composition superior in the appearance characteristics and the long-run workability as described above.
  • the resin composition of the present invention has superior appearance characteristics and the long-run workability in melt molding, and enables occurrence of yellowing etc., in melt molding to be inhibited particularly, even in melt molding at high temperatures of, for example, no less than 260°C.
  • a resin composition is produced according to the producing method of the present invention, the effects described above can be surely obtained.
  • various types of molded articles such as monolayered or multilayered films, sheets, pipes, containers and fibers superior in the appearance characteristics can be obtained.
  • Fig. 1 shows a schematic view illustrating a biaxial extruder used in Example 57.
  • the resin composition of the present invention contains (A) an ethylene-vinyl alcohol copolymer, (B) a carboxylic acid and/or a carboxylate ion and (C) a metal ion, and the component (B) includes (B2) a multivalent carboxylic acid and/or a multivalent carboxylate ion.
  • the resin composition may contain (D) a phosphate compound and (E) a boron compound as suitable components, and further may contain other optional component.
  • the carboxylate ion as the component (B) may form a salt with a counter cation such as the metal ion as the component (C), whereas the metal ion as the component (C) may form a salt with a counter anion such as the carboxylate ion as the component (B).
  • a counter cation such as the metal ion as the component (C)
  • a counter anion such as the carboxylate ion as the component (B).
  • the EVOH (A) is a principal component of the resin composition.
  • the EVOH (A) is a copolymer having an ethylene unit and a vinyl alcohol unit as principal structural units. It is to be noted that the EVOH may include one type or a plurality of types of other structural units except for the ethylene unit and the vinyl alcohol unit.
  • the EVOH is typically obtained by polymerizing ethylene and a vinyl ester, and saponifying the resulting ethylene-vinyl ester copolymer.
  • the lower limit of the ethylene content in the EVOH (i.e., the proportion of the number of ethylene units with respect to the total number of the monomer units in the EVOH) is preferably 20 mol %, more preferably 22 mol % and further preferably 24 mol %.
  • the upper limit of the ethylene content in the EVOH is preferably 60 mol %, more preferably 55 mol % and further preferably 50 mol %.
  • the ethylene content in the EVOH is smaller than the lower limit, for example, water resistance, hot water resistance and a gas barrier property under a high humidity when molded into a multilayered structure maybe impaired, or melt moldability may be deteriorated.
  • the ethylene content in the EVOH exceeds the upper limit, the gas barrier property when molded into a multilayered structure may be impaired.
  • the lower limit of a degree of saponification of the EVOH (i.e. , a proportion of the number of vinyl alcohol units with respect to the total number of vinyl alcohol units and vinyl ester units in the EVOH) is preferably 80 mol %, more preferably 95 mol % and further preferably 99 mol %.
  • the upper limit of the degree of saponification of the EVOH is preferably 100 mol % and more preferably 99.99 mol %.
  • the lower limit of the melt flow rate of the EVOH (in accordance with JIS-K7210, a measured value at a temperature of 210°C, under a load of 2160 g) is preferably 0.1 g/10 min, more preferably 0.5 g/10 min, further preferably 1 g/10 min and particularly preferably 3 g/10 min.
  • the upper limit of the melt flow rate in the EVOH is preferably 200 g/10 min, more preferably 50 g/10 min, further preferably 30 g/10 min, particularly preferably 15 g/10 min and further particularly preferably 10 g/10 min.
  • the carboxylic acid and/or the carboxylate ion contained in the resin composition is exemplified by (B1) a monocarboxylic acid and/or a monocarboxylate ion, and (B2) a multivalent carboxylic acid and/or a multivalent carboxylate ion.
  • the resin composition includes the multivalent carboxylic acid and/or the multivalent carboxylate ion (B2) as an essential component.
  • the monocarboxylic acid is a compound having one carboxyl group in a molecule.
  • the monocarboxylate ion is obtained by eliminating a proton in a carboxyl group of a monocarboxylic acid.
  • the content of the monocarboxylic acid and the monocarboxylate ion (B1) is, in light of reducing an odor, preferably less than 2 ⁇ mol/g, more preferably less than 1.5 ⁇ mol/g, further preferably less than 1.2 ⁇ mol/g and particularly preferably less than 1.0 ⁇ mol/g with respect to the total of the resin composition.
  • the content of the monocarboxylic acid falls within the range, the odor of the resin composition per se is reduced, and additionally the odor that is generated in melt molding of the resin composition is reduced, so that the operation environment is improved.
  • the odor that the molded product has after melt molding is reduced, so that the multilayered structure produced using the resin composition can be suitably used as a packaging material for even contents such as cooked rice and drinking water having a commercial value that is likely to be impaired particularly by generation of the odor.
  • the content of the monocarboxylic acid and the monocarboxylate ion (B1) is preferably no less than 2 ⁇ mol/g with respect to the total of the resin composition in light of quality stability, etc.
  • the content of the component (B1) is preferably no less than 2 . 5 ⁇ mol/g and more preferably no less than 3 ⁇ mol/g.
  • the resin composition having the content of the monocarboxylic acid and the monocarboxylate ion falling within the range enables the quantities of the component (B2) and the component (C) to be easily adjusted in producing the resin composition and products having stable quality to be easily obtained.
  • the monocarboxylic acid is not particularly limited, and examples thereof include formic acid, acetic acid, propionic acid, lactic acid, caproic acid, capric acid, acrylic acid, methacrylic acid, benzoic acid, 2-naphthoic acid, and the like. These monocarboxylic acids may have a hydroxyl group or a halogen atom.
  • the monocarboxylate ion is exemplified by an ion obtained by eliminating a proton in a carboxyl group in each of the monocarboxylic acids.
  • the pKa of the monocarboxylic acid is preferably no less than 3.5 and more preferably no less than 4 in light of an ability of adjusting the pH of the composition and melt moldability.
  • the multivalent carboxylic acid contained in the resin composition of the present invention is a compound having at least two carboxyl groups per molecule. It is to be noted that polymers are not included in the multivalent carboxylic acid.
  • the multivalent carboxylate ion is obtained by eliminating at least one of protons in carboxyl groups in a multivalent carboxylate acid. Due to containing the component (B2), the pH in the composition can be controlled and generation of gels and seeds in melt molding is reduced, and further occurrence of coloring such as yellowing resulting from a metal ion in melt molding can be reduced.
  • the occurrence of coloring such as yellowing can be inhibited due to including the multivalent carboxylic acid and/or the multivalent carboxylate ion as the component (B2) together with metal ion as the component (C) described later; however, it is believed that the inhibition may result from, for example, stable coordination of the multivalent carboxylic acid and the like with the metal ion that is reportedly a cause of yellowing, etc., thereby enabling incorporation of the metal ion.
  • the multivalent carboxylic acid and the like are present stably in the state of coordination with the metal ion in such a manner, whereby a catalytic function of the metal ion for a reaction such as yellowing of the EVOH can be inhibited, and as a result, occurrence of coloring such as yellowing also in melt molding at high temperatures can be inhibited.
  • the metal ion and the multivalent carboxylic acid, etc. are bonded by a comparatively weak interaction, so that only a small influence can be made on the interlayer adhesiveness in forming a multilayered structure; therefore, the resin composition of the present invention can achieve superior interlayer adhesiveness also in forming a multilayered structure.
  • the lower limit of the molar ratio (B2/C) of the content of the multivalent carboxylic acid and the multivalent carboxylate ion as the component (B2) (content in a dry resin composition) to the content of the component (C) is defined as 0.002, preferably 0.005, more preferably 0.01, further preferably 0.1 and particularly preferably 0.2.
  • the upper limit of the molar ratio is defined as 2, preferably 1.4, more preferably 1 and further preferably 0.6.
  • the ratio of content of the multivalent carboxylic acid and the multivalent carboxylate ion as the component (B2) to the content of the metal ion as the component (C) falls within the range, it is believed that the multivalent carboxylic acid can be sufficiently and stably coordinated with the metal ion, whereby coloring can be inhibited.
  • the molar ratio of less than the lower limit leads to failure in sufficient inhibition of the occurrence of yellowing, etc. by an influence of the metal ion, due to the small amount of the coordinated multivalent carboxylic acid.
  • the lower limit of the molar ratio (B2/C1) of the component (B2) to the component (C1) is preferably 0.002, more preferably 0.005, still more preferably 0.01, further preferably 0.1 and particularly preferably 0.2.
  • the upper limit of the molar ratio is preferably 2, more preferably 1.4, more preferably 1 and further preferably 0.6.
  • the lower limit of the specific content of the multivalent carboxylic acid and the multivalent carboxylate ion as the component (B2) is preferably 0.01 ⁇ mol/g, more preferably 0.05 ⁇ mol/g, further preferably 0.1 ⁇ mol/g and particularly preferably 0.5 ⁇ mol/g.
  • the upper limit of the content is preferably 20 ⁇ mol/g, more preferably 15 ⁇ mol/g, further preferably 10 ⁇ mol/g and particularly preferably 6 ⁇ mol/g.
  • an inhibitory effect of coloring such as yellowing may be small.
  • the appearance characteristics may be impaired (e.g. , gels and seeds are likely to be generated) and the long-run workability may be deteriorated (e.g., viscosity is increased by heating for a long time of period).
  • a general multivalent carboxylic acid is not particularly limited as long as it has at least two carboxyl groups per molecule and examples thereof include aliphatic dicarboxylic acids such as oxalic acid, malonic acid, succinic acid, maleic acid, fumaric acid, malic acid, glutaric acid, adipic acid and pimelic acid, aromatic dicarboxylic acids such as phthalic acid, isophthalic acid and terephthalic acid, tricarboxylic acids such as citric acid, isocitric acid and aconitic acid, carboxylic acids having at least four carboxyl groups such as 1,2,3,4-butanetetracarboxylic acid and ethylenediaminetetraacetic acid, hydroxycarboxylic acids such as citric acid, isocitric acid, tartaric acid, malic acid, mucic acid, tartronic acid and citramalic acid, ketocarboxylic acids such as oxaloacetic acid, mesoxalic acid, 2-ketoglu
  • the component (B2) is preferably a multivalent carboxylic acid and an anion thereof having at least one functional group selected from the set consisting of a hydroxy group, an amino group and a ketone group.
  • a functional group selected from the set consisting of a hydroxy group, an amino group and a ketone group.
  • stability in the state of coordination with the metal ion is enhanced, so that an ability of inhibiting occurrence of coloring in melt molding at a high temperature is enhanced.
  • a hydroxy group is more preferably included in light of appropriate adjustment of a coordination strength with the metal ion, whereby a multilayered structure superior in interlayer adhesiveness is obtained while inhibiting the occurrence of coloring.
  • the hydroxy group is preferably situated at an ⁇ -position with respect to the carboxyl group.
  • a multivalent carboxylic acid and multivalent carboxylate ion have a structure in which an elimination reaction of a water molecule is easily caused by an appropriate heating.
  • Such a multivalent carboxylic acid and the like are coordinated in the vicinity of the metal ion, whereas a coordinate binding force thereof can be weakened by an elimination reaction during heating in melt molding, and thus an ability of enhancing the interlayer adhesiveness by the alkali metal ion can be sufficiently achieved.
  • multivalent carboxylic acid and the like can maintain superior interlayer adhesiveness whereas occurrence of coloring resulting from the metal ion is reduced.
  • the multivalent carboxylic acid and the multivalent carboxylate ion include citric acid, isocitric acid, malic acid and the like, and anions thereof.
  • the component (B2) is a multivalent carboxylic acid in which at least a pair of carboxyl groups are linked each other via a linking group having 1 or 2 carbon atoms and an anion thereof.
  • a multivalent carboxylic acid and multivalent carboxylate ion one or a plurality of carboxyl groups can be coordinated with one metal ion in a highly sterically stable manner; therefore, a coordination state is considered to be stable as a complex.
  • coloring such as yellowing, etc. can be effectively suppressed, and other various functions can be also achieved with a good balance.
  • the linking group having 1 or 2 carbon atoms may include aliphatic linking groups such as an alkanediyl group, an alkanetriyl group and an alkenetriyl group, or aromatic linking groups such as a 1,2-benzenediyl group.
  • aliphatic linking groups such as an alkanediyl group, an alkanetriyl group and an alkenetriyl group
  • aromatic linking groups such as a 1,2-benzenediyl group.
  • Examples of such a type of multivalent carboxylic acid and multivalent carboxylate ion include citric acid, isocitric acid, malic acid, tartaric acid, malonic acid, succinic acid, itaconic acid, maleic acid, fumaric acid, tartronic acid, citramalic acid, aconitic acid, aspartic acid, 1,2,3,4-butanetetracarboxylic acid and the like, and anions thereof.
  • the component (B2) is preferably a multivalent carboxylic acid having at least three carboxyl groups like citric acid, isocitric acid, 1,2,3,4-butanetetracarboxylic acid, ethylene diamine tetraacetic acid and the like, and anions thereof. It is considered that due to using such a multivalent carboxylic acid and multivalent carboxylate ion, a coordination state with the alkali metal ion has electrically and sterically superior stability. As a result, superior coloring reducing function is suggested to be achieved.
  • the metal ion as the component (C) may involve a single type of metal or a plurality of types of metal. Due to including the metal ion in the resin composition of the present invention, interlayer adhesiveness can be enhanced in molding a multilayered structure, and as a result, durability of the multilayered structure can be enhanced. Although the reason why the metal ion enhances the interlayer adhesiveness is not necessarily clear, it is considered that affinity between hydroxy groups with one another in the EVOH is made higher between layers by the presence of the metal ions. In addition, in the case in which one of adjacent layers has a functional group capable of reacting with a hydroxy group in the EVOH in a molecule, it is also considered that the bond generation reaction is accelerated by the presence of the metal ion, etc.
  • the metal ion as the component (C) is exemplified by the alkali metal ion (C1), the alkaline earth metal ion (C2), and other transition metal ion, and the like.
  • the lower limit of the content of the metal ion (content in a dry resin composition) is preferably 2.5 ⁇ mol/g, more preferably 3.5 ⁇ mol/g and further preferably 4.5 ⁇ mol/g.
  • the upper limit of the content is preferably 22 ⁇ mol/g, more preferably 16 ⁇ mol/g and further preferably 10 ⁇ mol/g.
  • the metal ion as the component (C) preferably includes the alkali metal ion (C1).
  • the alkali metal ion include ions such as lithium, sodium, potassium, rubidium and cesium, and the ion of sodium or potassium is more preferable in light of industrial availability.
  • the component (C) includes the alkali metal ion, the long-run workability and interlayer adhesive strength in forming a multilayered structure are enhanced.
  • the alkali metal salt that gives the alkali metal ion as the component (C1) is not particularly limited, and is exemplified by aliphatic carboxylate salts, aromatic carboxylate salts, phosphate salts, and metal complexes, and the like, of such as lithium, sodium and potassium.
  • the alkali metal salt is, specifically, exemplified by sodium acetate, potassium acetate, sodium phosphate, lithium phosphorate, sodium stearate, potassium stearate, sodium salts of ethylenediaminetetraacetic acid, and the like. Of these, sodium acetate, potassium acetate and sodium phosphate are particularly preferable in light of availability.
  • the lower limit of the content of the alkali metal ion (C1) (content in a dry resin composition) is preferably 2.5 ⁇ mol/g, more preferably 3.5 ⁇ mol/g and further preferably 4.5 ⁇ mol/g.
  • the upper limit of the content is preferably 22 ⁇ mol/g, more preferably 16 ⁇ mol/g and further 10 ⁇ mol/g.
  • the component (C) includes the alkaline earth metal ion (C2).
  • the alkaline earth metal ion (C2) include ions of beryllium, magnesium, calcium, strontium, barium and the like, and ions of magnesium or calcium are more preferable in light of industrial availability.
  • the phosphate compound as the component (D) is contained in the resin composition of the present invention, thermal stability of the resin composition in melt molding can be enhanced. As a result, generation of gels and seeds is inhibited, thereby enabling improvement of the appearance characteristics.
  • the phosphate compound is not particularly limited and is exemplified by various types of oxo acids of phosphorus such as phosphoric acid and phosphorous acid, and salts thereof, and the like.
  • the phosphate salts may be contained in any forms such as a phosphate salt, a monohydrogen phosphate salt or a dihydrogen phosphate salt, and the type of counter cation thereof is not particularly limited, which is preferably an alkali metal or an alkaline earth metal and more preferably an alkali metal.
  • sodium dihydrogen phosphate, potassium dihydrogen phosphate, disodium hydrogen phosphate or dipotassium hydrogen phosphate is preferable in light of a large thermal stability improving effect.
  • the lower limit of the content of the phosphate compound (content in a value of phosphate radical in a dry resin composition) is preferably 5 ppm and further preferably 8 ppm.
  • the upper limit of the content of the phosphate compound is preferably 500 ppm, more preferably 200 ppm and further preferably 50 ppm.
  • the boron compound as the component (E) is contained in the resin composition of the present invention, thermal stability of the resin composition in melt molding can be enhanced. As a result, generation of gels and seeds is inhibited, thereby enabling improvement of the appearance characteristics.
  • the boron compound is blended with the resin composition, it is believed that a chelate compound is generated between the EVOH and the boron compound, and use of such a resin composition enables improvement of thermal stability and a mechanical properties compared with typical resin compositions.
  • the boron compound is not particularly limited and is exemplified by boric acids, boric acid esters, borate salts, boron hydrates, and the like.
  • the boric acids are exemplified by orthoboric acid (H 3 BO 3 ), metaboric acid, tetraboric acid and the like;
  • the boric acid esters are exemplified by triethyl borate, trimethyl borate and the like;
  • the borate salts are exemplified by alkali metal salts, alkaline earth metal salts of the foregoing various types of boric acids, borax, and the like.
  • orthoboric acid is preferable.
  • the lower limit of the content of the boron compound (content of boron compound in a value of boron element in a dry resin composition) is preferably 5 ppm, more preferably 10 ppm and further preferably 50 ppm.
  • the upper limit of the content of the boron compound is preferably 2,000 ppm, more preferably 1,000 ppm, further preferably 500 ppm and particularly preferably 300 ppm.
  • a plasticizer a stabilizer, a surfactant, a pigment, an ultraviolet ray absorbing agent, a slip agent, an antistatic agent, a drying agent, a crosslinking agent, a filler, a reinforcing agent such as various types of fibers can be also added in appropriate amounts, within the range not to impair the effects of the present invention.
  • thermoplastic resin other than the EVOH can be also blended in appropriate amounts, within the range not to impair the effects of the present invention.
  • thermoplastic resin any of various types of polyolefins (polyethylene, polypropylene, poly 1-butene, poly 4-methyl-1-pentene, an ethylene-propylene copolymer, a copolymer of ethylene and ⁇ -olefin having 4 or more carbon atoms, a copolymer of polyolefin and maleic anhydride, an ethylene-vinyl ester copolymer, an ethylene-acrylic acid ester copolymer, or a modified polyolefin obtained by graft modification of these with an unsaturated carboxylic acid or a derivative thereof, and the like), various types of nylons (nylon-6, nylon-66, nylon-6/66 copolymers, and the like), polyvinyl chloride, polyvinylidene chloride, polyester, polystyrene, polyacrylonit
  • the lower limit of the melt flow rate (a value measured at a temperature of 210°C, under a load of 2,160 g) of the resin composition of the present invention is preferably 0.1 g/10 min, further preferably 0.5 g/10 min, particularly preferably 1 g/10 min and further particularly preferably 3 g/10 min.
  • the upper limit of the melt flow rate of the resin composition is preferably 200 g/10 min, more preferably 50 g/10 min, further preferably 30 g/10 min, particularly preferably 15 g/10 min and further particularly preferably 10 g/10 min.
  • the resin composition of the present invention is molded into various types of molded articles such as films, sheets, containers, pipes and fibers by melt molding. These molded products can be also ground and molded again for the purpose of reuse. In addition, a film, a sheet, a fiber, and the like can be subjected to monoaxial orientation or biaxial orientation. As a melt molding process, extrusion molding, inflation extrusion, blow molding, melt spinning, injection molding, and the like can be employed.
  • the melt temperature in melt molding carried out using the resin composition of the present invention is preferably about 150 to 300°C.
  • the proportion of the alkali metal ions (C), and the multivalent carboxylic acid and multivalent carboxylate ion (B2) is adjusted as described above, so that occurrence of coloring such as yellowing can be inhibited not only in melt molding at a high temperature of no less than 200°C, but also in melt molding at a higher temperature of, for example, no less than 260°C.
  • the resin composition of the present invention can be effectively obtained by a producing method including, for example, a copolymerizing step in which ethylene and a vinyl ester are copolymerized to obtain an ethylene-vinyl ester copolymer (step 1), and a saponifying step in which the ethylene-vinyl ester copolymer is saponified to obtain an ethylene-vinyl alcohol copolymer (step 2), and further including a mixing step in which the ethylene-vinyl ester copolymer or the ethylene vinyl alcohol copolymer is mixed with (B2') a multivalent carboxylic acid and/or a salt thereof (step ⁇ ), later than the copolymerizing step.
  • a producing method including, for example, a copolymerizing step in which ethylene and a vinyl ester are copolymerized to obtain an ethylene-vinyl ester copolymer (step 1), and a saponifying step in which the ethylene-vinyl ester copolymer
  • the method for producing the resin composition mixing the component (B2') is carried out later than the copolymerizing step, so that a resin composition in which occurrence of yellowing, etc. in melt molding is inhibited can be obtained.
  • each step will be explained in detail.
  • the copolymerizing step includes copolymerization of ethylene and a vinyl ester, and subsequently a procedure in which unreacted ethylene and unreacted vinyl ester are removed to obtain an ethylene-vinyl ester copolymer solution as needed.
  • the component (B2') is added in the copolymerizing step, the resin composition finally obtained is not preferable in that an effect to inhibit coloring such as yellowing, i. e. , an effect predominantly intended by the present invention, is hardly achieved, or coloring may be rather enhanced.
  • a copolymerization process of ethylene with the vinyl ester is not particularly limited, and well-known methods such as, for example, solution polymerization, suspension polymerization, emulsion polymerization and bulk polymerization may be employed. Also, any of a continuous system and a batchwise system may be employed.
  • vinyl ester used in polymerization examples include vinyl formate, vinyl acetate, vinyl propionate, vinyl valerate, vinyl caprate, vinyl laurate, vinyl stearate, vinyl benzoate, vinyl pivalate and vinyl versatate, and vinyl acetate is suitably used in light of industrial availability and/or use of the same.
  • a copolymerizable monomer as a copolymerization component for example, alkene; an unsaturated acid such as acrylic acid, methacrylic acid, crotonic acid, maleic acid or itaconic acid, or an anhydride, a salt, a mono- or dialkyl ester thereof, or the like; nitrile such as acrylonitrile or methacrylonitrile; amide such as acrylamide or methacrylamide; olefin sulfonic acid such as vinylsulfonic acid, allylsulfonic acid or metaallylsulfonic acid, or a salt thereof; an alkylvinyl ether, vinyl ketone, N-vinylpyrrolidone, vinyl chloride, vinylidene chloride or the like may be also copolymerized in a small amount.
  • an unsaturated acid such as acrylic acid, methacrylic acid, crotonic acid, maleic acid or itaconic acid, or an anhydride,
  • a vinylsilane compound may be included in an amount of 0.0002 mol% or greater and 0.2 mol% or less as a copolymerization component.
  • the vinylsilane compound may include, for example, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltri( ⁇ -methoxy-ethoxy)silane, ⁇ -methacryloyloxypropylmethoxysilane or the like. Of these, vinyltrimethoxysilane, or vinyltriethoxysilane is suitably used.
  • the solvent used for polymerization is not particularly limited as long as it is an organic solvent capable of dissolving ethylene, a vinyl ester and the ethylene-vinyl ester copolymer.
  • a solvent for example, an alcohol such as methanol, ethanol, propanol, n-butanol or tert-butanol; dimethyl sulfoxide or the like may be used.
  • methanol is particularly preferable in light of ease in removal and separation after the reaction.
  • an azonitrile-derived initiator such as 2,2-azobisisobutyronitrile, 2,2-azobis-(2,4-dimethylvaleronitrile), 2,2-azobis-(4-methoxy-2,4-dimethylvaleronitrile) or 2,2-azobis-(2-cyclopropylpropionitrile); and organic peroxide-derived initiators such as isobutyryl peroxide, cumyl peroxyneodecanoate, diisopropyl peroxydicarbonate, di-n-propyl peroxydicarbonate, t-butyl peroxyneodecanoate, acetyl peroxide, lauroyl peroxide, benzoyl peroxide, t-butyl hydroperoxide, or the like may be used.
  • organic peroxide-derived initiators such as isobutyryl peroxide, cumyl peroxyneodecanoate, diisopropyl peroxydicarbonate, di-n-
  • the polymerization temperature is preferably 20 to 90°C and more preferably 40 to 70°C.
  • the polymerization time is preferably 2 to 15 hrs and more preferably 3 to 11 hrs.
  • the polymerization conversion is preferably 10 to 90% and more preferably 30 to 80% with respect to the vinyl ester charged.
  • the content of the resin in the solution after the polymerization is preferably 5 to 85% by mass and more preferably 20 to 70% by mass.
  • a polymerization inhibitor is added as needed, and unreacted ethylene gas is removed by evaporation, followed by removing an unreacted vinyl ester.
  • a process of removing an unreacted vinyl ester for example, a process including continuously supplying the copolymer solution at a constant rate through an upper part of a tower filled with Raschig ring, blowing therein an organic solvent vapor such as methanol through a lower part of the tower, distilling off mixed vapor of the organic solvent such as methanol and unreacted vinyl ester through the top of the tower, and taking out the copolymer solution from which the unreacted vinyl ester was removed through the bottom of the tower, or the like may be employed.
  • an alkali catalyst is added to the copolymer solution, and the copolymer is saponified.
  • a saponification process may be either continuous system, or a batchwise system.
  • the alkali catalyst for example, sodium hydroxide, potassium hydroxide, alkali metal alcoholate, or the like may be used.
  • Conditions of saponification may include, for example, in the case of batchwise system: the concentration of the copolymer solution being 10 to 50% by mass; the reaction temperature being 30 to 60°C; the amount of the catalyst used being 0.02 to 0.6 mol per mol of the vinyl ester structural unit; and the saponification time being 1 to 6 hrs.
  • a process in which the saponification reaction is carried out while efficiently removing a carboxylic acid methyl ester, and the like generated along with the saponification reaction using a conventionally well-known tower type reactor is preferable in that the amount of the alkali catalyst used can be reduced, whereas the reaction temperature is preferably 70 to 150°C and the amount of the catalyst used is preferably 0.001 to 0.2 mol per mol of vinyl ester structural unit in order to carry out the reaction in the state of a homogenous solution.
  • the EVOH yielded after completing the saponification reaction contains the alkali catalyst, byproduct salts such as sodium acetate and potassium acetate, and other impurities, these are preferably removed by neutralizing and washing as needed.
  • the EVOH after completing the saponification reaction is washed with water that scarcely contains metal ion, chloride ion and the like such as ion exchanged water, sodium acetate, potassium acetate and the like may partly remain.
  • the ethylene-vinyl ester copolymer obtained in the copolymerizing step or the ethylene vinyl alcohol copolymer obtained in the saponifying step is mixed with the multivalent carboxylic acid and/or a salt thereof (B2').
  • the multivalent carboxylic acid as the component (B2') is exemplified by the multivalent carboxylic acid exemplified above as the component (B2) of the resin composition.
  • a salt of the multivalent carboxylic acid as the component (B2') is exemplified by an alkali metal salt, an alkaline earth metal salt and the like of the multivalent carboxylic acid.
  • a method such as, for example, (1) a method of adding the component (B2') beforehand to a solution containing an ethylene-vinyl ester copolymer to be subjected to the saponifying step, (2) a method of adding the component (B2') during the saponification reaction of the ethylene-vinyl ester copolymer in the saponifying step, (3) a method of mixing with the component (B2') after obtaining the ethylene-vinyl alcohol copolymer in the saponifying step, or the like may be employed.
  • the mixing step is carried out later than the copolymerizing step as described above, and the mixing step is more preferably carried out in a system in which the concentration of the vinyl ester is no greater than 1,000 ppm.
  • the component (B2') is added to a system in which the concentration of the vinyl ester is greater than 1,000 ppm, an inhibitory effect of coloring such as yellowing is hardly achieved in the final resin composition, or coloring may be rather enhanced.
  • the mixing step is preferably carried out in the saponifying step described above.
  • carrying out the mixing step in the saponifying step is exemplified by methods such as (1) a method of adding the component (B2') beforehand to the ethylene-vinyl ester copolymer subjected to the saponifying step, (2) a method of adding the component (B2') during the saponification reaction of the ethylene-vinyl ester copolymer in the saponifying step, and the like.
  • the mixing step is carried out in the saponifying step, heat deterioration and the like that the EVOH may be subjected to during the producing step after the saponifying step are inhibited, whereby color characteristics is improved in forming a resin composition.
  • the saponification reaction of the ethylene-vinyl ester copolymer is typically carried out in a state where the ethylene-vinyl ester copolymer is dissolved in a solvent, so that the component (B') is preferably added in the form of a multivalent carboxylic acid dissolvable into the same solvent.
  • the method for producing the resin composition of the present invention in addition to the foregoing each step, further includes an pelletizing step in which a water-containing pellet of the ethylene-vinyl alcohol copolymer is obtained by an pelletizing operation from a solution including the ethylene-vinyl alcohol copolymer obtained in the saponifying step (step 3), and a drying step in which the water-containing pellet is dried to obtain a resin composition including the ethylene-vinyl alcohol copolymer (step 4), and the mixing step is carried out after the pelletizing step. Also according to the method, a resin composition with a reduced yellowing in melt molding can be efficiently obtained.
  • the ethylene-vinyl alcohol copolymer obtained by saponifying the ethylene-vinyl ester copolymer by the saponifying step is typically obtained in the form of a solution in which the copolymer is dissolved in a solvent including the solvent used in the saponification reaction.
  • a catalyst such as alkali used for the saponification reaction and sodium acetate that is generated as a byproduct, and the like are included, so that washing is carried out in order to remove them.
  • the ethylene-vinyl alcohol copolymer solution obtained in the saponifying step is pelletized to form a water-containing pellet of the EVOH.
  • the operation of the pelletizing for obtaining the water-containing pellet of the EVOH from the solution of the ethylene-vinyl alcohol copolymer in the pelletizing step is not particularly limited, and well-known methods may be used such as a method in which a cylindrical water-containing pellet of the EVOH is obtained by extruding the solution of the ethylene-vinyl alcohol copolymer into a coagulating bath including a cooled poor solvent to give a strand form followed by cooling and hardening and thereafter cutting using a strand cutter, or a method in which an ellipsoidal (go-stone-like) to spherical water-containing pellet of the EVOH is obtained by similarly extruding the solution of the ethylene-vinyl alcohol copolymer into a coagulating bath, immediately followed by cutting using a rotating blade, etc.
  • well-known methods may be used such as a method in which a cylindrical water-containing pellet of the EVOH is obtained by extruding the solution of the ethylene-vinyl
  • a method in which a water-containing pellet of the EVOH is obtained by bringing the solution of the ethylene-vinyl alcohol copolymer into contact with water vapor to previously give a water-containing resin composition of the EVOH followed by cutting according to a method described in Japanese Unexamined Patent Application, Publication No. 2002-121290 , or the like can be suitably used.
  • the moisture content in the water-containing pellet of the EVOH obtained by these methods is preferably 50 to 200% by mass, more preferably 60 to 180% by mass and further preferably 70 to 150% by mass on the basis of the dry weight of the EVOH.
  • the water-containing pellet of the EVOH obtained in the pelletizing step is preferably formed into a pellet of the resin composition including the EVOH finally by drying in the drying step.
  • the moisture content of the resin composition pellet after drying is preferably no greater than 1.0% by mass, more preferably no greater than 0.8% by mass and further preferably no greater than 0.5% by mass with respect to the total of the resin composition pellet for the purpose of preventing molding troubles such as generation of a void by foaming in a molding processing.
  • the method of drying the water-containing pellet of the EVOH is not particularly limited and well-known various types of methods can be used, and suitable examples of the methods include ventilation drying, fluidized drying and the like. These drying methods may be used either alone, or in combination of a plurality of the same, such as e.g., fluidized drying followed by ventilation drying. Drying treatment may be carried out by any method with a continuous system or a batchwise system. When a plurality of drying methods are carried out in combination, the continuous system or the batchwise system can be selected ad libitum for each drying method. Drying at a low oxygen concentration or in an oxygen-free state is also preferable in that deterioration of the resin composition by oxygen during drying can be reduced.
  • a method such as (1) a method of bringing the water-containing pellet of the EVOH into contact with a solution containing the component (B2'), or (2) a method of melting and kneading the water-containing pellet of the EVOH and the component (B2') in an extruder is suitably employed.
  • the component (B1), the component (C) and other components can be simultaneously mixed with the EVOH.
  • a method of immersing the water-containing pellet in a solution containing the component (B2') after the pelletizing step and before the drying step is preferable. According to the method, the component (B2') can be efficiently mixed in the resin composition and a resin composition with reduced yellowing in melt molding can be more effectively produced.
  • the water-containing pellet of the EVOH may have an arbitrary shape such as powder, granular, spherical or cylindrical chip-shaped.
  • any of methods by a batchwise system and a continuous system can be used.
  • the mass ratio (bath ratio) of the EVOH in the water-containing pellet to a solution containing each component is preferably no less than 3, more preferably no less than 10 and further preferably no less than 20.
  • any of conventionally well-known tower type apparatuses can be suitably used.
  • the immersion time is no less than 1 hour and preferably no less than 2 hrs.
  • each component to be contained in the resin composition may be immersed separately in a plurality of solutions in which each component is dissolved alone, or the immersion treatment may be carried out at once using a liquid in which a plurality of components are dissolved, and the immersion treatment is preferably carried out with a solution including all the components other than the EVOH in light of simplification of steps.
  • the each component When the solution containing each component other than the EVOH is obtained, the each component may be each independently dissolved in a solvent, but also a solution in which some components each other form a salt can be used.
  • concentration of each component in the solution is not particularly limited, and may be appropriately adjusted so that the intended content of each component is obtained in the finally obtained resin composition.
  • the solvent of the solution is not particularly limited, and water is preferable for a handling reason, etc.
  • the mixing step be carried out in the pelletizing step described above.
  • the mixing step enables the component (B2') to be homogeneously contained in the water-containing pellet of the EVOH. Accordingly, in the case in which the component (B2') is contained in the EVOH by immersing the water-containing pellet of the EVOH in a solution including the component (B2') later than the pelletizing step, there is an advantage that the immersion time can be shortened, and further color characteristics is improved in forming a resin composition.
  • the multilayered structure of the present invention is a multilayered structure provided with at least one layer obtained from the resin composition of the present invention.
  • the layer structure of the multilayered structure is not particularly limited; however, provided that: a layer obtained from the resin composition of the present invention is designated as E; a layer obtained from an adhesive resin is designated as Ad; and a layer obtained from a thermoplastic resin is designated as T, examples of the layer structure include T/E/T, E/Ad/T, T/Ad/E/Ad/T, and the like. Each layer of these may be either a monolayer, or a multilayer.
  • the method for producing the multilayered structure is not particularly limited. For example, a method of melt extruding a thermoplastic resin onto a molded product obtained from the resin composition of the present invention (film, sheet. etc.); a method of coextruding the resin composition of the present invention and other thermoplastic resin; a method of coinjecting the resin composition of the present invention with a thermoplastic resin; a method of laminating a molded article formed from the resin composition of the present invention and a film or a sheet of other base material using a well-known adhesive such as an organic titanium compound, an isocyanate compound or a polyester based compound; and the like may be exemplified.
  • a method of coextruding the resin composition of the present invention and other thermoplastic resin is preferably used.
  • the resin composition of the present invention is superior in long-run workability and appearance characteristics, and in particular, coloring is less likely to occur even if melted at a comparatively high temperature. Therefore, even if the resin composition of the present invention and other thermoplastic resin having a comparatively high melting temperature are coextruded, a multilayered structure being accompanied by suppressed occurrence of coloring such as yellowing, and being superior in the appearance can be obtained.
  • thermoplastic resin used for other layer in the multilayered structure examples include: homopolymers of an olefin or copolymers thereof such as linear low density polyethylene, low density polyethylene, medium density polyethylene, high density polyethylene, ethylene-vinyl acetate copolymers, ethylene-propylene copolymers, polypropylene, and propylene- ⁇ -olefin copolymers ( ⁇ -olefin having 4 to 20 carbon atoms), polybutene, polypentene; polyesters such as polyethylene terephthalate; polyamides such as polyester elastomers, nylon-6, and nylon-6,6; polystyrene, polyvinyl chloride, polyvinylidene chloride, acrylic resins, vinyl ester based resins, polyurethane elastomers, polycarbonate, chlorinated polyethylene, chlorinated polypropylene, and the like.
  • the aforementioned adhesive resin is not particularly limited as long as it has adhesiveness with the resin composition that includes EVOH of the present invention and the thermoplastic resin, but adhesive resins containing a carboxylic acid modified polyolefin are preferred.
  • a carboxylic acid modified polyolefin a carboxyl group-containing modified olefin-derived polymer can be suitably used which is obtained by allowing an ethylenic unsaturated carboxylic acid, an ester thereof or an anhydride of the same to be chemically bonded (for example, addition reaction, graft reaction, etc.) to an olefin-derived polymer.
  • the olefin-derived polymer as referred to herein means polyolefins such as polyethylene (low pressure, middle pressure, high pressure), linear low density polyethylene, polypropylene and polybutene, copolymers (for example, ethylene-vinyl acetate copolymers, ethylene-ethyl acrylate copolymers, etc.) of olefin and other monomer (vinyl ester, unsaturated carboxylate ester, etc.).
  • linear low density polyethylene ethylene-vinyl acetate copolymers (content of vinyl acetate being 5% by mass to 55% by mass) and ethylene-ethyl acrylate copolymers (content of ethyl acrylate being 8% by mass to 35% by mass) are preferred, and linear low density polyethylene and ethylene-vinyl acetate copolymers are particularly preferred.
  • ethylenic unsaturated carboxylic acid an ester thereof or an anhydride of the same, ethylenic unsaturated monocarboxylic acids, or esters thereof, ethylenic unsaturated dicarboxylic acids, or mono- or diesters thereof, or anhydrides of the same are exemplified, and of these, ethylenic unsaturated dicarboxylic acid anhydrides are preferred.
  • maleic acid, fumaric acid, itaconic acid, maleic anhydride, itaconic anhydride, maleic monomethyl ester, maleic monoethyl ester, maleic diethyl ester, fumaric monomethyl ester and the like are included, and particularly, maleic anhydride is suitable.
  • the amount of addition or grafting (i.e., degree of modification) of the ethylenic unsaturated carboxylic acid or an anhydride thereof to the olefin-derived polymer is 0.0001 to 15% by mass and preferably 0.001 to 10% by mass with respect to the olefin-derived polymer.
  • An addition reaction and a grafting reaction of the ethylenic unsaturated carboxylic acid or an anhydride thereof to the olefin-derived polymer can be carried out by, for example, a radical polymerization method, etc. in the presence of a solvent (e.g., xylene, etc.) and a catalyst (peroxide, etc.).
  • the melt flow rate (MFR) measured at 210°C of the carboxylic acid-modified polyolefin obtained in such a manner is preferably 0.2 to 30 g/10 min and further preferably 0.5 to 10 g/10 min.
  • These adhesive resins may be used either alone, or as a mixture of two types or more thereof.
  • thermoplastic resin etc.
  • a multimanifold-merging T die method, a feedblock-merging T die method, an inflation method, and the like may be exemplified.
  • molded articles films, sheets, tubes, bottles, etc.
  • the various types of molded articles include, for example, articles as in the following:
  • the secondary processing is not limited to each process illustrated for obtaining the molded article described above, and for example, any well-known secondary processing other than the aforementioned processes such as blow molding may be used ad libitum.
  • the multilayered structure has a layer obtained from an resin composition that is superior in appearance characteristics and long-run workability, it is accompanied by fewer fish eyes, gels and seeds (dirt under paint) and less coloring such as yellowing and thus, for example, can be suitably used as a food container and the like such as a deep draw container, a cup shape container, and a bottle.
  • the moisture content of the water-containing EVOH pellet was measured using a Halogen Moisture Analyzer "HR73" manufactured by Mettler-Toledo International Inc. under a conditions including a drying temperature of 180°C, a drying time of 20 min, a sample quantity of about 10 g.
  • the moisture content of the water-containing EVOH shown below is expressed as % by mass on the basis of dry EVOH.
  • Dry EVOH pellet was ground by freeze grinding.
  • resulting ground EVOH was sieved with a sieve having a nominal dimension of 1 mm (according to normal sieve standard JIS-Z8801).
  • EVOH powder passed through the sieve in an amount of 5 g was immersed in 100 g of ion exchanged water, and the mixture was stirred at 85°C for 4 hrs, followed by an operation of dewatering and drying repeated twice.
  • measurement of 1 H-NMR was carried out under the following measurement conditions, and the degree of saponification was determined by the analysis method described below.
  • an integrated value (I 1 ) of the peak of the chemical shift at 3.7 to 4 ppm, and an integrated value (I 2 ) of the peak of the chemical shift at 0.6 to 1.8 ppm were determined.
  • an integrated value (I 3 ) of the peak of the chemical shift at 3.1 to 3.7 ppm, an integrated value (I 4 ) of the peak of the chemical shift at 0.6 to 1.8 ppm, and an integrated value (I 5 ) of the peak of the chemical shift at 1.9 to 2.1 ppm were determined.
  • the dry EVOH pellet was ground by freeze grinding.
  • the ground EVOH obtained was sieved with a sieve having a nominal dimension of 1 mm (according to standard sieve specified in JIS-Z8801).
  • the EVOH powder in an amount of 10 g that passed through the sieve and 50 mL of ion exchanged water were charged into a 100 mL Erlenmeyer flask equipped with a stopper, then a cooling condenser was attached thereto, and the mixture was stirred at 95°C for 10 hrs, followed by extraction. Two mL of the resulting extraction liquid was diluted with 8 mL of ion exchanged water.
  • the diluted extraction liquid was subjected to quantitative analysis using ion chromatography "IC7000" manufactured by Yokogawa Electric Corporation to determine the amount of carboxylic acid and carboxylate ion, whereby the amount of carboxylic acid and carboxylate ion was calculated. It is to be noted that a calibration curve produced using an aqueous acetate solution was used in quantification. Ion chromatography measurement condition:
  • the dry EVOH pellet was ground by freeze grinding.
  • EVOH powder in an amount of 10 g and 50 mL of ion exchanged water were charged in a 100 mL stoppered Erlenmeyer flask equipped with a cooling condenser, and the mixture was stirred at 95°C for 10 hrs to execute heat extraction.
  • extract in a volume of 2 mL was diluted with 8 mL of ion exchanged water.
  • diluted extract was subjected to a quantitative analysis using an ICP emission spectrophotometer "Optima 4300 DV" manufactured by PerkinElmer Japan Co., Ltd., at each observation wavelength shown below, whereby the amount of each metal ion was quantitatively determined.
  • Ca 317.933 nm
  • the dry EVOH pellet was ground by freeze grinding.
  • EVOH powder in an amount of 1.0 g, 15 mL of concentrated nitric acid and 4 mL of concentrated sulfuric acid were charged into a stoppered 100 mL Erlenmeyer flask equipped with a cooling condenser to execute heat degradation at 200 to 230°C.
  • solution was diluted to 50 mL with ion exchanged water in a volumetric flask.
  • the solution was subjected to a quantitative analysis using an ICP emission spectrophotometer "Optima 4300 DV" manufactured by PerkinElmer Japan Co. , Ltd. , at an observation wavelength of 214.914 nm, whereby the amount of phosphorus element was quantitatively determined, and the amount of phosphate compounds was calculated to give a value of phosphate radical.
  • a dry EVOH pellet provided as a sample in an amount of 50 mg was completely combusted by an oxygen flask combustion method, and thus resultant combusted ash deposition was dissolved in 10 mL of a 1 mol/L aqueous nitric acid solution.
  • the solution was subjected to a quantitative analysis using an ICP emission spectrophotometer "Optima 4300 DV" manufactured by PerkinElmer Japan Co., Ltd., at an observation wavelength of 249.667 nm, whereby the content of boron compounds was obtained in a value of boron element.
  • Each dried EVOH pellet obtained in Examples and Comparative Examples in an amount of 5 g was heated and melted at 220°C and 260°C for 2 min in a heat compression press apparatus to produce disk-shaped samples having a thickness of 2 mm.
  • the state of coloring of the obtained disk-shaped samples were visually confirmed and evaluated as in the following.
  • Extrusion temperature 180/ 260/ 260/ 260°C (feeding zone/ compression zone/ metering zone/ die) Screw rotation speed: 40 rpm
  • Output rate 1.3 kg/hr Chill roll temperature: 80°C Winding speed: 3.1 m/min Film thickness: 20 ⁇ m
  • the monolayer film produced by the method described above was rolled up around a paper tube and the degree of coloring on the edge of the film roll was evaluated visually as in the following.
  • Extrusion temperature 180/ 210/ 210/ 210°C (feeding zone/ compression zone/ metering zone/ die) Screw rotation speed: 40 rpm Output rate: 1.3 kg/hr Number of die holes: 2
  • LLDPE linear low-density polyethylene
  • Ad adhesive resin
  • MD machine direction
  • TD transverse direction
  • the internal temperature of the polymerization bath was adjusted to 60°C
  • 362 mL of the initiator solution was injected to initiate polymerization.
  • ethylene was introduced to maintain the reactor pressure of 3.6 MPa and the polymerization temperature of 60°C, and the initiator solution was continuously added at 1,120 mL/hr using the aforementioned initiator solution to perform polymerization.
  • the polymerization was stopped by cooling when the polymerization conversion reached 40%.
  • nitrogen gas was bubbled to completely eliminate ethylene.
  • the resulting copolymer solution was continuously supplied through an upper part of a tower filled with Raschig ring, and methanol vapor was blown through a lower part of the tower.
  • EVAc solution was added methanol to adjust a concentration of 15% by mass.
  • EVAc 38 kg of EVAc in the solution
  • 76.6 L of an alkali solution 10% by mass NaOH solution in methanol, molar ratio (MR) relative to vinyl acetate units in EVAc: 0.4
  • the reaction liquid was neutralized by adding 9. 2 kg of acetic acid and 60 L of water to terminate the reaction.
  • the neutralized reaction liquid was transferred from the reactor to a metal drum, and left to stand at room temperature for 16 hrs, thereby permitting cooling and hardening to give a cake form. Thereafter, liquid was removed from the resin in the cake form using a centrifugal separator ("H-130" manufactured by Kokusan Centrifuge Co., Ltd., number of revolution: 1,200 rpm). Next, a step of washing the resin with water was conducted for 10 hrs in which washing was carried out while continuously supplying ion exchanged water to the central portion of the centrifugal separator from above. The conductivity of the washing liquid after 10 hrs from starting washing was 30 ⁇ S/cm (measured with "CM-30ET” manufactured by TOA Electronics Ltd.).
  • the EVOH in the form of powder obtained in this manner was dried using a dryer at 60°C for 48 hrs.
  • the stirring was stopped, and the temperature of the dissolving vessel was lowered to 65°C.
  • degassing of the water/ methanol solution of EVOH was carried out.
  • water-containing EVOH pellet in an amount of 40 kg and 150 L of ion exchanged water were placed in a metal drum having a height of 900 mm and an opening diameter of 600 mm. An operation of washing at 25°C for 2 hrs while stirring, and dewatering the liquid was repeated twice. Next, 150 L of 1 g/L aqueous acetic acid solution was added to 30 kg of the water-containing EVOH pellet, and an operation of washing at 25°C for 2 hrs while stirring, and dewatering the liquid was repeated twice.
  • a water-containing EVOH pellet (w-EVOH-1) was obtained from which impurities such as byproducts in the saponifying step had been removed.
  • the conductivity of the washing liquid after carrying out the sixth washing was measured with "CM-30ET" manufactured by TOA Electronics Ltd., and as a result, the washing liquid was revealed to have a conductivity of 3 ⁇ S/cm.
  • CM-30ET manufactured by TOA Electronics Ltd.
  • a methanol solution of the EVAc from which unreacted vinyl acetate had been removed was obtained according to an operation similar to Synthesis Example 1 except that: the amounts of vinyl acetate and methanol charged in polymerization of the ethylene-vinyl acetate copolymer were changed to 85.2 kg and 32.3 kg, respectively; the pressure in the reaction tank was changed to 2.9 MPa; the amount of the initiator solution (methanol solution of AMV having a concentration of 2.5 g/L) injected upon initiation of the polymerization was changed to 310 mL; and the amount of the initiator solution continuously added was changed to 950 mL/hr in Synthesis Example 1.
  • the reaction time of the polymerization reaction was 5 hrs and the polymerization conversion was 40%.
  • a methanol solution of the EVAc from which unreacted vinyl acetate had been removed was obtained according to an operation similar to Synthesis Example 1 except that: the amounts of vinyl acetate and methanol charged in polymerization of the ethylene-vinyl acetate copolymer were changed to 76.7 kg and 11.0 kg, respectively; the pressure in the reaction tank was changed to 5.5 MPa; the amount of the initiator solution (methanol solution of AMV having a concentration of 2.5 g/L) injected upon initiation of the polymerization was changed to 510 mL; and the amount of the initiator solution continuously added was changed to 1, 570 mL/hr in Synthesis Example 1. The reaction time of the polymerization reaction was 5 hrs and the polymerization conversion was 40%.
  • a methanol solution of the EVAc from which unreacted vinyl acetate had been removed was obtained according to an operation similar to Synthesis Example 1 except that: the amounts of vinyl acetate and methanol charged in polymerization of the ethylene-vinyl acetate copolymer were changed to 102.0 kg and 17.7 kg, respectively; the pressure in the reaction tank was changed to 2.9 MPa; the amount of the initiator solution (methanol solution of AMV having a concentration of 2.5 g/L) injected upon initiation of the polymerization was changed to 280 mL; and the amount of the initiator solution continuously added was changed to 850 mL/hr in Synthesis Example 1.
  • the reaction time of the polymerization reaction was 5 hrs and the polymerization conversion was 40%.
  • the EVOH-1 When EVOH-1 was analyzed for the ethylene content and the degree of saponification according to the procedure described above, the ethylene content (Et) was 32 mol % and the degree of saponification (DS) was no less than 99.98 mol %.
  • the EVOH-1 contained 2.6 ⁇ mol/g of citric acid and citrate ion as the multivalent carboxylic acid and multivalent carboxylate ion (B2), 7.0 ⁇ mol/g of sodium ion as the metal ion (C), 10 ppm of the phosphate compound (D) in a value of phosphate radical, and 156 ppm of the boron compound (E) in a value of boron element.
  • the EVOH resin composition pellets (EVOH-2 to 31, and 34 to 44) were obtained in a similar manner to Example 1 except that the type of the water-containing EVOH pellet, and the type and amount of each compound blended with the aqueous solution were changed as shown in Table 1 and Table 4.
  • the obtained each EVOH resin composition was analyzed and evaluated in a manner similar to Example 1.
  • the results of the analysis of the ethylene content, etc. are shown in Table 2 and Table 5, and the results of the evaluation of the coloring resistance, etc. are shown in Table 3 and Table 6.
  • a water-containing EVOH pellet (w-EVOH-5) was obtained similarly to Synthesis Example 1 except that 30 g of "N,N'-hexamethylenebis(3,5-di-t-butyl-4-hydroxy-hydrocinnamamide)" (Irganox 1098, manufactured by Ciba Specialty Chemicals) that is an antioxidant was added when the EVOH was dissolved in the water/methanol mixed solution in the pelletizing step in the Synthesis Example 1 and thereafter purification was carried out according to an operation similar to Example 1. Furthermore, a pellet of a dry EVOH resin composition (EVOH-32) was obtained according to an operation similar to Example 1 except that w-EVOH-5 was used in place of w-EVOH-1.
  • EVOH-32 dry EVOH resin composition
  • a water-containing EVOH pellet (w-EVOH-6) was obtained similarly to Example 32 except that the amount of "N,N'-hexamethylenebis(3,5-di-t-butyl-4-hydroxy-hydrocinnamamide)" added was changed to 5 g, followed by purification according to an operation similar to Example 32. Furthermore, a pellet of a dry EVOH resin composition (EVOH-33) was obtained according to an operation similar to Example 1 except that w-EVOH-6 was used in place of w-EVOH-1.
  • the water-containing EVOH pellet after the immersion was deawatered using centrifugal dehydrator, and then dried in a hot-air dryer at 80°C for 3 hrs, followed by drying at 120°C for 24 hrs to obtain a pellet of a dry EVOH resin composition (EVOH-45).
  • the EVOH-45 When EVOH-45 was analyzed for the ethylene content and the degree of saponification according to the procedure described above, the ethylene content was 32 mol % and the degree of saponification was no less than 99.98 mol %.
  • the EVOH-45 contained 3.2 ⁇ mol/g of citric acid and citrate ion as the multivalent carboxylic acid and multivalent carboxylate ion (B2), 2.9 ⁇ mol/g of magnesium ion as the metal ion (C), 10 ppm of the phosphate compound (D) in a value of phosphate radical, and 156 ppm of the boron compound (E) in a value of boron element.
  • the EVOH resin composition pellets (EVOH-46 to 60) were obtained in a similar manner to Example 34 except that the type of the water-containing EVOH pellet, and the type and amount of each compound blended with the aqueous solution were changed as shown in Table 7.
  • the obtained each EVOH resin composition was analyzed and evaluated in a manner similar to Example 34.
  • the results of the analysis of the ethylene content, etc. are shown in Table 8, and the results of the evaluation of the coloring resistance, etc. are shown in Table 9.
  • the water-containing EVOH pellet after the immersion was dewatered using centrifugal dehydrator, and then dried in a hot-air dryer at 80°C for 3 hrs, followed by drying at 120°C for 24 hrs to obtain a pellet of a dry EVOH resin composition (EVOH-1).
  • the EVOH-61 When EVOH-61 was analyzed for the ethylene content and the degree of saponification according to the procedure described above, the ethylene content was 32 mol % and the degree of saponification was no less than 99.98 mol %.
  • the EVOH-61 contained 16.7 ⁇ mol/g of acetate ion as the monocarboxylic acid and monocarboxylate ion (B1), 0.1 ⁇ mol/g of citric acid and citrate ion as the multivalent carboxylic acid and multivalent carboxylate ion (B2), 7.4 ⁇ mol/g of sodium ion as the metal ion (C), 10 ppm of the phosphate compound (D) in a value of phosphate radical, and 156 ppm of the boron compound (E) in a value of boron element.
  • the EVOH resin composition pellets (EVOH-62 to 73) were obtained in a similar manner to Example 46 except that the type of the water-containing EVOH pellet, and the type and amount of each compound blended with the aqueous solution were changed as shown in Table 10.
  • the obtained each EVOH resin composition was analyzed and evaluated in a manner similar to Example 46.
  • the results of the analysis of the ethylene content, etc. are shown in Table 11, and the results of the evaluation of the coloring resistance, etc. are shown in Table 12.
  • a water-containing EVOH pellet (w-EVOH-7) was obtained similarly to Synthesis Example 1 except that 22 g of citric acid was further added in neutralizing and stopping the reaction by adding acetic acid and water in the saponifying step in the Synthesis Example 1 and thereafter washing, pelletizing and purification were carried out according to an operation similar to Example 1. Furthermore, a pellet of a dry EVOH resin composition (EVOH-74) was obtained according to an operation similar to Example 1 except that w-EVOH-7 was used in place of w-EVOH-1.
  • a water-containing EVOH pellet (w-EVOH-8) was obtained similarly to Synthesis Example 1 except that 2 g of citric acid was added when the EVOH was dissolved in the water/methanol mixed solution in the pelletizing step in the Synthesis Example 1 and thereafter purification was carried out according to an operation similar to Example 1. Furthermore, a pellet of a dry EVOH resin composition (EVOH-75) was obtained according to an operation similar to Example 1 except that w-EVOH-8 was used in place of w-EVOH-1.
  • the w-EVOH-1 obtained in Synthesis Example 1 was dried in a hot-air dryer at 80°C for 1 hour, whereby a water-containing EVOH pellet having a moisture content of 50% by mass was obtained.
  • the obtained water-containing EVOH pellet was charged into a biaxial extruder (details shown below) at a rate of 10 kg/hr, then the temperature of the resin in a discharge opening was adjusted to 100°C, and an aqueous solution including 0.63 g/L citric acid, 6.74 g/L trisodium citrate, 0.11 g/L phosphoric acid and 9.9 g/L boric acid was added at a rate of 0.6 L/hr from a solution adding part at a tip part on the discharge opening side shown in Fig.
  • the strand-shaped and melted water-containing EVOH discharged from a dice was cut by a strand cutter to obtain a cylindrical water-containing EVOH pellet (moisture content: 25% by mass).
  • the obtained water-containing EVOH pellet was dried in a hot-air dryer at 80°C for 1 hour, followed by consequently drying at 120°C for 24 hrs to obtain a pellet of dry EVOH resin composition (EVOH-76).
  • a water-containing EVOH pellet (w-EVOH-9) was obtained by carrying out saponification, washing, pelletizing and purification according to an operation similar to Synthesis Example 1 except that 101 g of vinyl acetate (400 ppm with respect to the methanol solution having a concentration of 15% of EVAc) and 27 g of trisodium citrate were added to the methanol solution having a concentration of 15% by mass of EVAc used for the saponifying step, and that an alkali solution was added after the mixture was stirred to permit homogenous dissolution in Synthesis Example 1. Furthermore, a pellet of a dry EVOH resin composition (EVOH-77) was obtained according to an operation similar to Example 1 except that w-EVOH-9 was used in place of w-EVOH-1.
  • a water-containing EVOH pellet (w-EVOH-10) was obtained by carrying out saponification, washing, pelletizing and purification according to an operation similar to Example 57 except that the amount of vinyl acetate added was changed to 152 g (600 ppm with respect to the methanol solution having a concentration of 15% of EVAc) in Example 58. Furthermore, a pellet of the dry EVOH resin composition (EVOH-78) was obtained according to an operation similar to Example 1 except that w-EVOH-10 was used in place of w-EVOH-1.
  • a water-containing EVOH pellet (w-EVOH-11) was obtained by carrying out polymerization, saponification, washing, pelletizing and purification according to an operation similar to Synthesis Example 1 except that 48 g of citric acid was further added when vinyl acetate and methanol were charged into the reaction tank in the polymerization step in Synthesis Example 1. Furthermore, a pellet of a dry EVOH resin composition (EVOH-79) was obtained according to an operation similar to Comparative Example 1 except that w-EVOH-11 was used in place of w-EVOH-1.
  • the dry EVOH resin composition pellets EVOH-74 to -79 obtained in Examples 55 to 59 and Comparative Example 20 were analyzed and evaluated in a manner similar to Example 1.
  • the results of the analysis of the ethylene content, etc. and the evaluation of coloring resistance, etc. are shown in Table 13 and Table 14.
  • Et DS (B1) (B2) (C) (B2) / (C) (D) (E)
  • Example 55 EVOH-74 32 99.98 - - citric acid 2.6 Na 7.0 0.371 10 156 890
  • Example 56 EVOH-75 32 99.98 - - citric acid 2.6 Na 7.0 0.371 10 156 890
  • Example 57 EVOH-76 32 99.98 - - citric acid 2.6 Na 7.0 0.371 10 156 890
  • Example 59 EVOH-78 32 99.98 - - citric acid 2.6 Na 7.0
  • the EVOH resin composition of the present invention can be suitably used as a material for various types of molded articles such as monolayered or multilayered films, sheets, pipes, containers and fibers superior in the appearance characteristics since the EVOH resin composition of the present invention is superior in appearance characteristics and long-run workability, and enables occurrence of coloring such as yellowing to be inhibited even by melt molding at high temperatures, particularly, for example, a high temperature of no less than 260°C.

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Claims (22)

  1. Composition de résine comprenant :
    (A) un copolymère d'éthylène-alcool vinylique ;
    (B) au moins un choisi parmi l'ensemble constitué par un acide carboxylique et un ion carboxylate ; et
    (C) un ion de métal ;
    dans laquelle
    le composant (B) comprend (B2) au moins un choisi dans l'ensemble constitué par un acide carboxylique multivalent et un ion carboxylate multivalent,
    au moins une paire de groupes carboxyle dans le composant (B2) est liée l'un à l'autre par l'intermédiaire d'un groupe de liaison contenant 1 ou 2 atome(s) de carbone, et
    le rapport molaire (B2/C) de l'acide carboxylique multivalent et de l'ion carboxylate multivalent (B2) sur l'ion de métal (C) est de 0,002 ou plus et 2 ou moins.
  2. Composition de résine selon la revendication 1, dans laquelle la teneur en composant (B2) est de 0,01 µmol/g ou plus et 20 µmol/g ou moins.
  3. Composition de résine selon la revendication 1 ou 2, dans laquelle le composant (B2) contient au moins un type de groupe fonctionnel choisi dans l'ensemble constitué par un groupe hydroxy, un groupe amino et un groupe cétone.
  4. Composition de résine selon la revendication 3, dans laquelle le composant (B2) contient un groupe hydroxy.
  5. Composition de résine selon l'une quelconque des revendications 1 à 4, dans laquelle le composant (B2) contient au moins trois groupes carboxyle.
  6. Composition de résine selon l'une quelconque des revendications 1 à 5, dans laquelle la teneur en composant (C) est de 2,5 µmol/g ou plus et 22 µmol/g ou moins.
  7. Composition de résine selon l'une quelconque des revendications 1 à 6, dans laquelle le composant (C) comprend (C1) un ion de métal alcalin.
  8. Composition de résine selon la revendication 7, dans laquelle la teneur en composant (C1) est de 2,5 µmol/g ou plus et 22 µmol/g ou moins.
  9. Composition de résine selon la revendication 7 ou 8, dans laquelle le rapport molaire (B2/C1) du composant (B2) sur le composant (C1) est de 0,002 ou plus et 2 ou moins.
  10. Composition de résine selon l'une quelconque des revendications 1 à 9, dans laquelle le composant (C) comprend (C2) un ion de métal alcalino-terreux.
  11. Composition de résine selon l'une quelconque des revendications 1 à 10, la composition de résine comprenant en outre (D) un composé de phosphate,
    dans laquelle la teneur en composé de phosphate (D) est de 5 ppm ou plus et 500 ppm ou moins en termes de valeur de radical phosphate.
  12. Composition de résine selon l'une quelconque des revendications 1 à 11, la composition de résine comprenant en outre (E) un composé de bore,
    dans laquelle la teneur en composé de bore (E) est de 5 ppm ou plus et 2000 ppm ou moins en termes de valeur d'élément de bore.
  13. Composition de résine selon l'une quelconque des revendications 1 à 12, dans laquelle la teneur en (B1) acide monocarboxylique et ion monocarboxylate en tant que composant (B) est inférieure à 2 µmol/g.
  14. Composition de résine selon l'une quelconque des revendications 1 à 12, le composant (B) comprenant en outre (B1) au moins un choisi dans l'ensemble constitué par un acide monocarboxylique et un ion mono-carboxylate,
    dans laquelle la teneur en acide monocarboxylique et en ion monocarboxylate (B1) n'est pas inférieure à 2 µmol/g.
  15. Composition de résine selon l'une quelconque des revendications 1 à 14, la composition de résine étant destinée à être utilisée dans un moulage par co-extrusion.
  16. Procédé de production de la composition de résine selon l'une quelconque des revendications 1 à 15, le procédé comprenant
    une étape de copolymérisation dans laquelle de l'éthylène et un ester de vinyle sont copolymérisés pour obtenir un copolymère d'éthylène-ester de vinyle, et
    une étape de saponification dans laquelle le copolymère d'éthylène-ester de vinyle est saponifié pour obtenir un copolymère d'éthylène-alcool vinylique, et
    le procédé comprenant en outre
    une étape de mélange dans laquelle le copolymère d'éthylène-ester de vinyle ou le copolymère d'éthylène alcool vinylique est mélangé avec (B2') au moins un parmi un acide carboxylique multivalent ou un sel de celui-ci, après l'étape de copolymérisation.
  17. Procédé de production de la composition de résine selon la revendication 16, dans lequel l'étape de mélange est réalisée dans un système dans lequel la concentration en ester de vinyle n'est pas supérieure à 1000 ppm.
  18. Procédé de production de la composition de résine selon la revendication 16 ou 17, le procédé comprenant en outre :
    une étape de formation de pastille dans laquelle une pastille contenant de l'eau d'un copolymère d'éthylène-alcool vinylique est obtenue par une opération de formation de pastille à partir d'une solution comprenant le copolymère d'éthylène-alcool vinylique obtenu dans l'étape de saponification ; et
    une étape de séchage dans laquelle la pastille contenant de l'eau est séchée pour obtenir une composition de résine comprenant un copolymère d'éthylène-alcool vinylique,
    dans lequel l'étape de mélange est réalisée après l'étape de formation de pastille.
  19. Procédé de production de la composition de résine selon la revendication 18, dans lequel l'étape de mélange est réalisée entre l'étape de formation de pastille et l'étape de séchage par immersion de la pastille contenant de l'eau dans une solution contenant le composant (B2').
  20. Procédé de production de la composition de résine selon la revendication 18, dans lequel l'étape de mélange est réalisée dans l'étape de formation de pastille.
  21. Procédé de production de la composition de résine selon la revendication 16 ou 17, dans lequel l'étape de mélange est réalisée dans l'étape de saponification.
  22. Structure multicouche pourvue d'au moins une couche obtenue à partir de la composition de résine selon l'une quelconque des revendications 1 à 15.
EP11759453.1A 2010-03-25 2011-03-23 Composition de résine, son procédé de production et structure multicouche Active EP2551300B1 (fr)

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JP7504628B2 (ja) * 2020-03-04 2024-06-24 株式会社クラレ エチレン－ビニルアルコール共重合体含有樹脂組成物及び成形体
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IL243111B (en) 2018-06-28
JP5808460B2 (ja) 2015-11-10
IL243110A (en) 2017-11-30
SG10201502313WA (en) 2015-05-28
SG184248A1 (en) 2012-11-29
JP2014177644A (ja) 2014-09-25
IL222079A (en) 2016-09-29
TWI488907B (zh) 2015-06-21
CN102803378B (zh) 2015-07-29
CA2794192A1 (fr) 2011-09-29
SG10201502314UA (en) 2015-05-28
EP2551300A4 (fr) 2014-05-14
KR101795094B1 (ko) 2017-11-07
KR20130040189A (ko) 2013-04-23
JP2014111793A (ja) 2014-06-19
US9073293B2 (en) 2015-07-07
CN102803378A (zh) 2012-11-28
RU2012145281A (ru) 2014-04-27
RU2599297C2 (ru) 2016-10-10
CA2794192C (fr) 2019-02-19
EP2551300A1 (fr) 2013-01-30
BR112012024220B1 (pt) 2020-01-14
US20130018133A1 (en) 2013-01-17
WO2011118648A1 (fr) 2011-09-29
JP5824088B2 (ja) 2015-11-25
TW201202333A (en) 2012-01-16
JP5619874B2 (ja) 2014-11-05
JPWO2011118648A1 (ja) 2013-07-04

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